The natural occurrence of Pandora heteropterae (Zygomycetes: Entomophthorales) infecting Lygus lineolaris (Hemiptera: Miridae)

An unknown fungal pathogen was recovered from Lygus lineolaris (Palisot de Beauvois) during a survey of parasitic and pathogenic natural enemies conducted in Franklin County, Arkansas. The pathogen was identified as Pandora heteropterae (Ba?azy) Keller based on characteristics of the morphology, as well as growth and sporulation on hosts. The fungus infected 11 of the 3405 (0.32%) wild L. lineolaris collected. In a laboratory host-range bioassay, five of seven hemipteran species from the families Miridae, Coreidae, Lygaeidae, and Pentatomidae were successfully infected. P. heteropterae was previously reported only once, from an unidentified host species in Poland. Here we describe the morphology and growth of P. heteropterae and discuss its potential impact on L. lineolaris in the field.     

The evolution of root hairs and rhizoids

Background

Almost all land plants develop tip-growing filamentous cells at the interface between the plant and substrate (the soil). Root hairs form on the surface of roots of sporophytes (the multicellular diploid phase of the life cycle) in vascular plants. Rhizoids develop on the free-living gametophytes of vascular and non-vascular plants and on both gametophytes and sporophytes of the extinct rhyniophytes. Extant lycophytes (clubmosses and quillworts) and monilophytes (ferns and horsetails) develop both free-living gametophytes and free-living sporophytes. These gametophytes and sporophytes grow in close contact with the soil and develop rhizoids and root hairs, respectively.

Scope

Here we review the development and function of rhizoids and root hairs in extant groups of land plants. Root hairs are important for the uptake of nutrients with limited mobility in the soil such as phosphate. Rhizoids have a variety of functions including water transport and adhesion to surfaces in some mosses and liverworts.

Conclusions

A similar gene regulatory network controls the development of rhizoids in moss gametophytes and root hairs on the roots of vascular plant sporophytes. It is likely that this gene regulatory network first operated in the gametophyte of the earliest land plants. We propose that later it functioned in sporophytes as the diploid phase evolved a free-living habit and developed an interface with the soil. This transference of gene function from gametophyte to sporophyte could provide a mechanism that, at least in part, explains the increase in morphological diversity of sporophytes that occurred during the radiation of land plants in the Devonian Period.     

Comparative phosphate acquisition in giant-celled rhizophytic algae (Bryopsidales, Chlorophyta): Fleshy vs. calcified forms

Phosphate uptake through above-ground thalli vs. subterranean rhizoids has been compared in siphonaceous rhizophytic green algal species from five globally distributed tropical genera: Avrainvillea nigricans Decaisne, Caulerpa lanuginosa J. Agardh, Halimeda incrassata (J. Ellis) J.V. Lamouroux, Penicillus capitatus Lamarck, and Udotea flabellum (J. Ellis & Solander) M. Howe. Plants were collected, acclimated to lab conditions for 3 days, and then incubated for 8 h at saturating light intensity with 30 μM PO₄³⁻ added to their above-ground thallus or below-ground rhizoids. Percent tissue phosphorus was then compared to control specimens, which were run simultaneously in the absence of phosphate. The two fleshy species, A. nigricans and C. lanuginosa, showed no significant differences in tissue nutrient status, and displayed much larger variation among controls than the three calcified species. Calcified species showed greater phosphorus content after being exposed to either above- or below-ground thallus portions, indicating that these seaweeds can respond to short term increases in nutrient availability and have a more regulated nutrient acquisition mechanism. Results suggest that calcification may play an important role in phosphorus absorption.     

Rhizoid differentiation of <Emphasis Type="Italic">Spirogyra</Emphasis> is regulated by substratum

Some species of Spirogyra can anchor to substratum with rod- or rosette-shaped rhizoid (hapteron). The rhizoid differentiation can be induced by cutting algal filaments in a laboratory. Requirement of contact stimulation for rhizoid differentiation has been reported (Nagata in Plant Cell Physiol 14:531-541, 1973a). However, the control mechanism of rhizoid morphology has not been elucidated. When cut filaments were incubated on the glass surface, start of tip growth, secretion of lectin-binding material and callose synthesis were observed. In the absence of contact to the glass surface, none of above phenomena was induced. Systematic analysis showed that rosette-shaped rhizoid was formed only on the hydrophobic substratum. On the hydrophobic substratum, both Bandeiraea (Griffonia) simplicifolia lectin and jacalin strongly stained the rhizoids. On the hydrophilic substratum, however, only Bandeiraea (Griffonia) simplicifolia lectin strongly stained the rhizoids.